Conveyor system for clinical test apparatus

ABSTRACT

The conveyor system for clinical test apparatus includes a main transport conveyor and a plurality of auxiliary conveyors located alongside the main transport conveyor. The auxiliary conveyors define straight line paths of travel parallel to the straight line paths of travel of the main conveyor. Each of the auxiliary conveyors is operated by drive means separate from the main transport conveyor. Two crossover points are provided between the main transport conveyor and the auxiliary conveyor. One crossover point is an entrance from the main transport conveyor to the auxiliary conveyor and the other crossover point is an exit from the auxiliary conveyor to the main transport conveyor. Each crossover point is controlled by a gate. One of the gates is a divert gate which can be actuated to block the main transport path thereby diverting puck traffic onto the auxiliary conveyor. The other gate is an interface gate which is used primarily to read information on a sample tube before it is introduced into a test apparatus and also functions as a load and unload station for the clinical test apparatus. The conveyor system also has a main unload and load system wherein tubes that have been completely tested are removed from pucks and reloaded with new tubes that are to be tested.

BACKGROUND OF THE INVENTION

This invention relates to conveyor devices for transporting biological material in containers to clinical test apparatus and more particularly to a conveyor system with a main transport lane for all containers to be tested and individual sidebar lanes associated with different clinical test apparatus, and traffic control gates at each sidebar lane for diverting separate groups of containers to their corresponding clinical test apparatus.

The term "clinical testing" is intended to refer to hematological tests, tests relating to immunoassay, toxicology, urinalysis and any other specific category of testing performed on biological or body material such as blood, serum, and urine for example. The clinical testing of blood, serum, urine or other body fluid provides invaluable information relative to the health status of an individual and clinical test results are commonly used for diagnostic evaluation, surgical decision making and the recognition of when a change or changes have occurred in a patient's health status.

Clinical testing often involves esoteric and costly procedures that must produce quality information with a high degree of accuracy. As new clinical tests are conceived and conventional clinical tests are improved, the expanding pool of information that is obtainable from various clinical tests must be weighed against the cost of obtaining such information. By reducing the cost of clinical tests, such tests can have the widest possible availability to those individuals who would benefit most from the tests.

One known way of reducing the costs for clinical testing is to perform such tests automatically and as quickly as possible. Thus diverse clinical test apparatus have been developed which operate independently of each other to perform different types of specialized tests with a minimal amount of personnel. The tests are usually performed on fluid samples that are contained in sample tubes, although other containment formats are also used, especially when the test material is not in fluid form.

However separate personnel and supervision teams are generally required to oversee each individual clinical test apparatus and separate work areas are often required for each specific category of clinical test apparatus. Thus, a laboratory which is engaged in diverse clinical testing procedures would require a relatively large facility space to accommodate the separate clinical test apparatus.

In a further attempt to reduce operating costs for clinical testing a common transport system has been developed to automatically deliver test material containers such as sample tubes to a variety of otherwise unrelated and independent clinical test apparatus. Such transport system includes a conveyor adapted to run along a predetermined travel path with different, unrelated clinical test apparatus located along the travel path of the conveyor. Each of the clinical test apparatus is adapted to operate on a common sample tube that is transported by the conveyor system.

The known conveyor systems for delivering sample tubes to different clinical apparatus are usually custom built for the particular needs of a test laboratory. In many instances the construction of conveyor systems for clinical test apparatus require dedicated installations of electrical power supply, plumbing service, vacuum and pressure service. Thus the known conveyor systems usually have the character of custom design, permanency and inflexibility once they are installed.

It is thus desirable to provide a conveyor system for clinical testing of biological materials in containers, which conveyor system can be constructed with modular stations for each clinical test apparatus, with simplified installations for plumbing, electricity, vacuum and pressure service that do not require ground, wall or ceiling installation.

OBJECTS AND SUMMARY OF THE INVENTION

Among the several objects of the invention may be noted the provision of a novel conveyor system for clinical test apparatus, a novel conveyor system that has a main transport lane and one or more auxiliary lanes corresponding to each clinical apparatus, a novel conveyor system for clinical test apparatus wherein auxiliary transport lanes are provided alongside main transport lanes for side by side movement of sample tubes on a main transport lane and on an auxiliary transport lane, a novel conveyor system for clinical test apparatus including a main transport conveyor and a plurality of separately run auxiliary conveyors, and wherein each auxiliary conveyor is associated with a separate clinical test apparatus, a novel conveyor system wherein each auxiliary conveyor is provided with traffic control gates including a diverter gate and an interface gate wherein the diverter gate selectively diverts sample tubes from the main transport conveyor to the auxiliary conveyor and the interface gate controls return of the diverted sample tubes to the main transport conveyor, a novel conveyor system for clinical test apparatus that also carries its own utility service lines such as electrical, plumbing, pressure and vacuum lines, a novel conveyor system for clinical test apparatus wherein the main transport conveyor is separately driven by one motor while the auxiliary transport conveyors are each driven by separate motors, and novel gates for directing sample tubes to selected clinical apparatus for testing or other functional purpose.

Other objects and features of the invention will be in part apparent and in part pointed out hereinafter.

In accordance with the present invention, the conveyor system for clinical test apparatus includes a main transport conveyor that defines a closed circuit travel path. The closed circuit travel path permits objects that remain on the conveyor to repeat the travel path when the conveyor moves in one direction. The main transport conveyor has straight line paths and curved paths. The conveyor system also includes a plurality of auxiliary conveyors that define a straight line travel path. The auxiliary conveyors, which are arranged in series with one another are located alongside the straight line travel paths of the main transport conveyor. Each auxiliary conveyor transports an object from one end of the auxiliary conveyor to the other end without retracing any point of travel when the auxiliary conveyor is moving in one direction, which is normally the same direction as the main transport conveyor.

Each of the auxiliary conveyors are controlled by separate motors or drive means that are preferably independent of the motor or drive means for the main transport conveyor. In this manner the auxiliary conveyors can be arranged as modules alongside the main transport conveyor.

Separation means are provided between the main transport conveyor and the auxiliary conveyor except at predetermined intersections between the main transport conveyor and the auxiliary conveyor. Such intersections are defined by gate controlled crossover openings that permit diversion of sample tubes from the main transport conveyor to the auxiliary conveyor and vice versa.

One of the gate openings is controlled by a divert gate device which has actuatable diversion means for diverting movement of objects on the main transport conveyor to the auxiliary conveyor. The diversion means has one position that blocks off the flow of traffic on the main transport conveyor and at the same time directs such traffic to the auxiliary conveyor. The diversion means has another position that does not interfere with traffic on the main transport conveyor and thus permits such traffic to bypass the auxiliary conveyor.

Another crossover opening that provides a direct flow path from the auxiliary conveyor to the transport conveyor is controlled by an interface gate device that is located upstream of the crossover opening. The interface gate device as well as the divert gate device cooperate with label readers for the sample tubes. The sample tubes are thus rotated at each gate device to enable the label reader to obtain a reading of the sample tube label.

A clinical test apparatus or other functional device which operates on the sample tubes is associated with each auxiliary conveyor. Thus one auxiliary conveyor can be associated with a load and unload station for the sample tubes. Other auxiliary conveyors are respectively associated with different clinical test apparatus that perform different categories of tests on sample tubes.

If a sample tube is to be tested by a specific clinical test apparatus the system programming and the information on the individual sample tube label will cause activation of the gates in a manner which will direct the sample tube to the intended clinical test apparatus while enabling sample tubes that are not intended to be tested by a clinical test apparatus to bypass the auxiliary conveyor associated with that clinical test apparatus. Thus the sample tubes will go only to a clinical test apparatus that is to perform a required test on the sample tube.

Sample tubes are unloaded from pucks when they are to be tested by a clinical test apparatus. The empty puck is reloaded with another sample tube that is exiting from the test apparatus. Thus the puck remains on the conveyor during unloading and reloading of sample tubes. The unloading and reloading of the pucks is accomplished by a robotic device that forms no part of the present invention.

Although the main transport conveyor and the auxiliary transport conveyors are separately driven and each clinical test apparatus operates independently of the other clinical test apparatus, the movement of all sample tubes and the operation of all the gates in the conveyor system is governed by a single process control means such as a computer.

Columns which support the conveyor system also support utility service for the conveyor system such as electrical lines, plumbing lines, air pressure lines and vacuum lines. The installation of such utility lines above ground and on the conveyor columns facilitates servicing and construction of the conveyor system.

The invention accordingly comprises the constructions hereinafter described, the scope of the invention being indicated in the claims.

DESCRIPTION OF THE DRAWINGS

In the drawings,

FIG. 1 is a simplified schematic plan view of a conveyor system incorporating the present invention;

FIG. 2 is an enlarged simplified schematic plan view thereof with a reduced number of auxiliary conveyors;

FIG. 3 is a front elevational view thereof;

FIG. 4 is a sectional view thereof taken on the line 4--4 of FIG. 3;

FIG. 5 is an enlarged schematic plan view of a divert gate device employed in the conveyor system;

FIG. 6 is an enlarged schematic plan view of an interface gate device employed in the conveyor system;

FIG. 7 is a sectional view taken on the line 7--7 of FIG. 6;

FIG. 8 is a sectional view taken on the line 8--8 of FIG. 6;

FIG. 9 is a fragmentary elevational view of the support structure for the conveyor system;

FIG. 10 is a sectional view taken on the line 10--10 of FIG. 9; and,

FIG. 11 is a sectional view taken on the line 11--11 of FIG. 9.

Corresponding reference characters indicate corresponding parts throughout the several views of the drawings.

DETAILED DESCRIPTION OF THE INVENTION

A conveyor system for clinical test apparatus incorporating one embodiment of the invention is generally indicated by the reference number 10.

Referring to FIG. 1 the conveyor system 10 includes a main transport conveyor 12 defining a closed circuit travel path in a generally horizontal plane. The closed circuit travel path permits objects that remain on the conveyor 12 to repeat the path of travel when the conveyor 12 is moving in one direction. The closed circuit travel path includes two straight line paths 16 and 18 and two curved paths 22 and 24 at respective opposite ends of the straight line paths 16 and 18.

An auxiliary conveyor 30, which has a straight line travel path, is positioned alongside and parallel to the straight line travel path 16 of the main transport conveyor 12. The straight line travel path of the auxiliary conveyor 30 permits objects on the conveyor 30 to move from one point to another without retracing any point of travel when the conveyor 30 is moving in one direction.

The auxiliary conveyor 30 is associated with a load and unload station 40 that represents an initial and final transport point for sample tubes 106. Robots (not shown) at the station 40 remove tested sample tubes 106 from the conveyor 30 and replaces them with new sample tubes 106 to be tested. An auxiliary conveyor 32 is associated with a clinical test apparatus station 42 which performs a specific category of tests on a sample tube 106. Additional auxiliary conveyors 34, 36, 38 and 39, similar to the conveyors 30 and 32 are also provided alongside and parallel to the straight line paths 16 and 18 of the conveyor 12 in series with the auxiliary conveyors 30 and 32. Each auxiliary conveyor 34, 36, 38 and 39 is associated with a clinical test apparatus station such as 44, 46, 48 and 49 that perform separate and distinct categories of clinical tests. However the auxiliary conveyors 30-39 associated with the different stations 40-49 are generally similar in operation and construction.

The main transport conveyor 12 is arranged to run in a counterclockwise direction, although the direction of travel is a matter of choice. The auxiliary conveyor 30, and all other auxiliary conveyors 32-39 preferably run in the same direction as the main transport conveyor 12. The auxiliary conveyor 30, which has an upstream end 50 and a downstream end 52, travels in a generally horizontal plane that is preferably coplanar with the travel plane of the main transport conveyor 12. Pairs of gate devices 160 and 170 are provided on the conveyor system 10 between opposite ends 50 and 52 of any of the auxiliary conveyors 30-39.

For purposes of clarity, reference will be made to a simplified conveyor system as shown in FIG. 2 which has the same operating structures as the conveyor system 10 of FIG. 1, but is more clearly illustrated on a larger scale than that of FIG. 1.

The main transport conveyor 12 includes a known conveyor belt 60. The conveyor belt 60 defines a main transport lane also indicated by the reference number 60 since the main transport lane is the path traveled by objects on the conveyor belt 60. The conveyor belt 60 is bordered at opposite sides by edge walls 68 and 70 that are generally mirror images of each other. The edge walls 68 and 70 include ledge portions 76 and 78 (FIG. 4) located at a predetermined height above the conveyor belt 60 and projecting over the conveyor belt 60. The ledge portions 76 and 78 cooperate with the conveyor belt 60 to form a vertical confinement for generally cylindrical sample tube pucks 100 that travel on the conveyor belt 60 and hold a sample tube 106, which can be of different heights and diameter within a predetermined size range such as approximately 13 to 16 mm in diameter and 75 to 100 mm in height.

The puck 100 includes resilient biasing means 104 (FIG. 6) which apply a slight retention force on the sample tube 106. The puck 100 maintains a stable positioning of the sample tube 106 as the conveyor belt 60 transports the puck 100 from one location to another along the conveyor belt travel path. The biasing means 104 in the puck 100 permits removal and replacement of the sample tube 106 in the puck 100 as often as is necessary. As used herein the term sample tube 106 is generally intended to include the puck 100 which holds the sample tube 106, unless otherwise indicated.

The auxiliary conveyor 30 includes a known conveyor belt 120. The conveyor belt 120 defines a sidebar lane also indicated by the reference number 120 since the sidebar lane is the path traveled by objects on the conveyor belt 120. The conveyor belt 120 is bordered on opposite sides by edge walls 128 and 130 (FIG. 4) similar to the edge walls 68 and 70. The edge walls 128 and 130 include ledge portions 136 and 138 which perform the same function as the ledge portions 76 and 78.

As most clearly shown in FIG. 4 the edge walls 70 and 130 are located adjacent each other between the edge walls 68 and 128. The adjacent edge walls 70 and 130 function as a separation or segregation means between the main transport lane 60 and the sidebar lane 120. The adjacent edge walls 70 and 130 include a sidebar entrance opening 146 (FIG. 2) proximate the upstream end 50 of the auxiliary conveyor 30 and a sidebar exit opening 148 proximate the downstream end 52 of the auxiliary conveyor 30. The entrance opening 146 and the exit opening 148 are also referred to as traffic intersections that are controlled by the gate devices 160 and 170.

The gate device 160, which is also referred to as a divert gate, is provided at the edge wall 68 of the transport conveyor 12 in substantial alignment with the sidebar entrance opening 146 at the upstream end 50 of the auxiliary conveyor 30. The gate device 170 which is also referred to as an interface gate is provided alongside the edge wall 128 of the auxiliary conveyor 30 a short distance upstream of the sidebar exit opening 148.

In order to efficiently control puck traffic at the intersections 146 and 148 between the main transport lane 60 and any of the sidebar lanes 120 the gate devices 160 and 170 must obtain a reading of information pertaining to each sample tube 106 passing through the gate device. Subsequent action on the sample tube 106 including a determination of the travel path, and the unloading and/or loading of the sample tubes 106 in the pucks 100 will be based on the information that is read from the sample tube 106 at the gates 160 and 170.

Each sample tube 106 is a reservoir of sample fluid that is later extracted or withdrawn from the sample tube at the clinical test apparatus in selected quantities for whatever tests are to be performed by one or more clinical test apparatus. Each sample tube 106 thus includes a label 108 (FIG. 7) with information relating to the identity of the individual supplying the test sample, the type of fluid in the sample tube and the type of test or tests that are to be performed on the material contained in the sample tube, hereinafter referred to as the label information. Under this arrangement each sample tube 106 is uniquely distinguishable from other sample tubes and can be individually identified. The label 108 applied to the sample tube 106 is preferably in a machine readable format such as a known bar code that can be automatically read or interpreted in a known manner by a known label reading device.

Thus a label reader device at the gates 160 and 170 will read the sample tube label and communicate the label information to a system control computer (not shown) that governs all processing operations performed by the conveyor system 10 and also governs the acceptance of the sample tubes 106 by the respective clinical test apparatus. The process control computer thus retains the label information and process activity information for each sample tube 106. This information is specifically used to control the gate devices 160 and 170 to direct the sample tube 106 to the appropriate clinical test apparatus in accordance with known programming techniques.

With regard to the control of puck traffic at the auxiliary conveyor 30, the divert gate 160 (FIG. 5) includes three pneumatically controlled plunger devices 180, 182 and 184 of known construction supported on a gate housing 186. The plunger devices 180 and 182 respectively include retractable fingers 192 and 194, and the plunger device 184 includes a retractable divert head 196 with an inclined surface 198. A puck rotating mechanism 190 is provided on the gate housing 186 between the plunger devices 180 and 182 to rotate the puck 100 and the sample tube 106 to allow the sample tube label 108 to be read by a known label scanner or reader device 200 (FIG. 7) shown at the gate 170 but also provided at the gate 160.

When the respective fingers 192 and 194 of the plunger devices 180 and 182 are in a protracted position as shown in FIG. 5 the combination of the plunger devices 180 and 182 with the puck rotating mechanism 190 constitute a singulator device that enables the label reader device 200 to read the label of one sample tube 106 at a time. The retractable fingers 192 and 194 are spaced apart a distance slightly larger than the puck diameter to permit the puck rotating mechanism 190 to rotate the puck 100 between the protracted fingers 192 and 194.

The puck rotating mechanism 190, which can be automatically controlled in a known manner for slight lateral movement toward and away from the main transport lane 60, includes a puck contacting belt 206 driven by wheels 208 and 210. When a singulated sample tube 106 has been read by the reader device 200, the finger 194 retracts to permit the singulated sample tube 106 to move toward the plunger device 184. The finger 192 remains protracted to hold back the non-singulated sample tubes 106. The protracted or retracted position of the divert head 196 will determine whether the singulated sample tube 106 stays on the main transport lane 60 or is diverted to the sidebar lane 120. Retracted positions of the fingers 192, 194 and the divert head 196 are shown dotted in FIG. 5.

If all testing has been completed for the singulated sample tube 106 the divert head 196 (FIG. 5) will be protracted to block off the main transport lane 60. The singulated sample tube 106 will thus be diverted to the sidebar lane 120 of the auxiliary conveyor 30, which leads to the load/unload station 40. Completely tested singulated sample tube 106 will travel on the sidebar lane 120 to the interface gate 170. If further testing is required for the singulated sample tube 106 the divert head 196 will be retracted to enable the sample tube 106 to remain on the main transport lane 60 and thereby bypass the auxiliary conveyor 30 and the load/unload station 40.

When another sample tube 106 is to be singulated for label reading at the divert gate 160 the finger 194 is protracted and the finger 192 is retracted to permit the line of sample tubes 106 to proceed to the finger 194. The finger 192 is then protracted to singulate the next sample tube 106.

The interface gate 170 (FIG. 6) includes three pneumatically controlled plunger devices 220, 222 and 224 of known construction supported on a gate housing 226. The plunger devices 220, 222 and 224 respectively include retractable fingers 232, 234 and 236. Retracted positions of the fingers 232, 234 and 236 are shown dotted in FIG. 6.

One puck rotating mechanism 242, similar to the puck rotating mechanism 190 is supported on the gate housing 226 between the plunger devices 220 and 222 and another puck rotating mechanism 244, similar to the puck rotating mechanism 190 is supported on the gate housing 226 between the plunger devices 222 and 224. The combination of the plunger devices 220 and 222 with the puck rotating mechanism 242 constitute a singulator device that enables the label reader device 200 at the gate 170 (FIG. 7) to read the label 108 of one sample tube 106 at a time, in the same manner as described for the singulator device at the divert gate 160.

The completely tested sample tube 106 is thus lined up with other sample tubes 106 behind the protracted finger 234 of the plunger device 222 at the interface gate 170 while the finger 232 of the plunger device 220 is retracted. The retracted finger 232 of the plunger device 220 is then protracted to singulate sample tube 106, wherein the sample tube 106 is confined between the fingers 232 and 234 for rotation by the puck rotating mechanism 242. The label 108 (FIG. 7) on the rotating sample tube 106 is read by the reader device 200. The process or system control computer (not shown) that is linked to each of the label reader devices 200 maintains a history of the test activity for each and every sample tube 106 and a record of all testing not yet performed on any sample tube.

If there is a confirmation at the interface gate 170 that all testing has been completed for a singulated sample tube 106 as determined during the label reading operation at the puck rotating mechanism 242, then the sample tube 106 is withdrawn from the puck 100 by a robot (not shown) while the puck 100 is singulated at the puck rotating mechanism 242. The unloaded puck 100 with exposed biasing spring 104 (FIG. 6) remains on the auxiliary conveyor 30 due to the vertical confinement provided by the ledges 136 and 138 (FIG. 4) at the conveyor edge portions 128 and 130.

The unloaded puck 100 (FIG. 6) is then allowed to pass beyond the singulation point by retraction of the finger 234. The unloaded puck 100 is held from further movement by the protracted finger 236 at the plunger device 224. A robot (not shown) places a new sample tube 106 in the unloaded puck 100 while the puck is restrained by the finger 236. The new sample tube 106 in the reloaded puck 100 is rotated by the rotating mechanism 244 to permit an initial reading of test instructions and sample identification from the label of the new sample tube 106. The rotating mechanisms 242 and 244 can have separate drive means or be commonly driven from a single drive means.

The finger 236 of the interface gate 170 is then retracted to permit the new sample tube 106 to proceed through the sidebar exit opening 148 (FIG. 2) to transfer from the sidebar lane 120 of the auxiliary conveyor 30 to the main transport lane 60. Other pucks 100 that are lined up for singulation at the interface gate 170 of the auxiliary conveyor 30 are similarly processed for reading of their respective sample tube labels. Thus, sample tubes 106 at the interface gate 170 of the auxiliary conveyor 30 will be unloaded if their testing is completed or allowed to pass beyond the gate 170 if further testing is indicated by the label reader 200.

The newly loaded sample tubes 106 and the older retained sample tubes 106 that still require further testing pass through the interface gate 170 (FIG. 2) at the load/unload station 40 and exit at the exit opening 148 from the auxiliary conveyor 30 to the main transport lane 60. The main transport lane 60 carries the sample tubes 106 to the divert gate 160 at the intersection of the auxiliary conveyor 32 and the main transport lane 60. The sample tubes 106 are initially held in line at the divert gate 160 by the protracted finger 194 (FIG. 5). The sample tubes 106 are then singulated for label reading in a manner similar to that previously described for the divert gate 160 at the auxiliary conveyor 30.

When the label of a singulated sample tube 106 has been read the process computer receives the information and will cause the plunger device 184 to protract the divert head 196 if the sample tube 106 is to be tested by the clinical apparatus 42 that is associated with the auxiliary conveyor 32. Protraction of the divert head 196 will block off the main transport lane 60 and direct the sample tube 106 onto the sidebar lane 120 of the auxiliary conveyor 32.

If the label for the sample tube 106 at the divert gate 160 of the auxiliary conveyor 32 indicates that the sample tube 106 is not to be tested by the clinical apparatus associated with the auxiliary conveyor 32 the process control computer will cause the divert head 196 to be retracted. With the divert head 196 in a retracted position the sample tube 106 will continue to travel on the main transport lane 60 thereby bypassing the auxiliary conveyor 32 and the clinical apparatus 42.

Assuming the sample tube 106 is to be tested at the clinical apparatus 42 such sample tube 106 will be diverted onto the sidebar lane 120 which moves the sample tube 106 to the interface gate 170. The sample tube 106 is held in line at the interface gate 170 by the protracted finger 234 (FIG. 4) which holds sample tube 106 and other sample tubes 106 in line for singulation and label reading in a manner as previously described with respect to the interface gate 170 at the auxiliary conveyor 30. Label reading at the interface gate 170 is used to confirm that the sample tube 106 is to be tested by the clinical test apparatus 42.

Once the confirmatory reading has been taken at the interface gate 170 of the auxiliary conveyor 32, a robot (not shown) will remove the sample tube 106 from its singulation position for transfer to the clinical test apparatus 42. The unloaded puck 102 remains on the auxiliary conveyor 132 due to the vertical confinement provided by the ledges 136 and 138 (FIG. 4) at the conveyor edge portions 128 and 130. The plunger device 222 (FIG. 6) is then activated to retract the finger 234 and permit the unloaded puck 102 to travel to the next protracted finger 236 where it is held back by the finger 236 at the next puck rotating mechanism 244. The unloaded puck 102 is then reloaded with a sample tube 106 that has already been tested at the clinical test apparatus 42.

It should be noted that the sample tube 106 that was robotically removed from the puck 100 at the singulator mechanism for transfer to the clinical test apparatus 42 is generally not the same sample tube 106 that is loaded in the empty puck 102 when the empty puck 102 is at the rotating mechanism 244. The unloading of the sample tube 106 from a puck 100 and the reloading of the puck 100 with a different sample tube 106 is due to the clinical test apparatus 42 being operated in continuous fashion.

Thus the clinical test apparatus 42 receives input sample tubes 106 to be tested simultaneously as it delivers output sample tubes 106 that have been tested. The label of the sample tube 106 that is at the puck rotating mechanism 244 is read by the label reader device at the puck rotating mechanism 244 and provides information to the process computer that the sample tube 106 has been tested at the clinical test apparatus 42. The plunger device 224 is then activated to retract the finger 236 and permit the sidebar lane 120 of the auxiliary conveyor 32 to move the sample tube 106 through the exit opening 148 of the interface gate 170 onto the main transport lane 60 in the direction of the clinical test apparatus.

The main transport lane 60 will carry the sample tube 106 to the next intersection that is governed by the next divert gate 160, namely the auxiliary conveyor 34 that is associated with the clinical test apparatus 44. Depending upon the information on the label 108 of the sample tube 106 and the information stored in the process control computer memory, the sample tube 106 will be either diverted onto the auxiliary conveyor 34 or allowed to stay on the main transport lane 60. If the sample tube 106 does not require any further testing it will not be diverted to any other auxiliary conveyors associated with clinical test apparatus and will usually be diverted to the auxiliary conveyor 30 for unloading at the unload station 40.

Each of the auxiliary conveyors 30-39 are powered by separate and independent motor devices. Thus the inclusion of additional auxiliary conveyors into the conveyor system 10 can be easily accomplished since the adjacent edge walls 70 and 130 of the main conveyor and the auxiliary conveyor can be detachably fastened together in any suitable known manner. Furthermore, the extrusions which form the edge walls 68, 70, 128 and 130 can be formed in standard sizes with and without the exit and entrance openings 146 and 148 to facilitate the addition of any other auxiliary conveyors.

If desired, auxiliary conveyors can be provided not only for transfer of tubes to clinical test apparatus but also for transfer of tubes to stations that perform other functions that may be considered beneficial for the processing of the sample tubes. For example, the next sequential station 42 from the load and unload station 40 rather than being associated with a clinical test apparatus can be used as a label check station for the purpose of checking whether a sample tube label 108 has a proper bar code, whether the label 108 has been properly affixed to the sample tube 106 and whether any other identification function is lacking in connection with the sample tube. The label check station will operate to remove any questionable sample tubes 106 from the conveyor system for remediation or disposal. The label check station will also operate to confirm that a sample tube has been properly labeled, and upon such confirmation the sample tube will be returned to the main transport lane 60.

The main transport conveyor 12 and the auxiliary conveyors 30-39 are commonly supported on identical column members 260 (FIGS. 9-11) that are spaced a predetermined distance from each other. Bracket members 270 (FIG. 4) are provided near an upper end of each of the columns 260 to join the edge wall 68 of the conveyor 12 to the column 260. The adjacent edge walls 70 and 130 are integrally joined in any suitable known manner, such as by fasteners (not shown). In addition a joining member 274, which supports the conveyor 12, joins the edge wall 68 to the edge wall 70. Another joining member 276, which supports the auxiliary conveyors 30-39, and is similar to the joining member 274, joins the edge wall 128 to the edge wall 130. Thus the bracket members 270 extending from the column members 260 support the conveyers 12 and 30-39 as well as the respective edge walls 68, 70, 128 and 130 in cantilever arrangement with respect to the column members 260.

It will be noted that the edge walls 68, 70, 128 and 130 as well as the bracket members 270 and the joining members 274 and 276 can each be formed as extrusions of predetermined length.

Service support brackets 290 (FIG. 9) are joined to the column members 260 between the bracket members 270 and a base portion 300 of the column members 260. The service support brackets hold boxes 306 for electrical service, conduits 308 for air pressure, conduits 310 for vacuum service and conduits 312 for plumbing service to the conveyor system 10 and to any of the clinical test apparatus associated with the conveyor system 10. Any suitable known valving or switches are provided on the conduits 306-312 to control the utility service to the conveyor system 10.

Some advantages of the invention evident from the foregoing description include a conveyor system having a main transport lane and a sidebar lane that are substantially parallel to each other and operate side-by-side, a novel conveyor system which includes a main transport conveyor that runs in an endless circuit and auxiliary conveyors provided alongside the main conveyor at the straight line paths of the main conveyor to permit crossover between the main conveyor and the auxiliary conveyor and vice versa, a novel conveyor system wherein the main conveyor and auxiliary conveyors are each powered by separate motors, a novel conveyor system wherein the main conveyor and the auxiliary conveyor can be built as modules to permit inclusion of any selected number of auxiliary conveyors as well as the elimination of unwanted auxiliary conveyors should they no longer be needed at some future time, a novel conveyor system having traffic control gates that can be positioned directly alongside the main conveyor and the auxiliary conveyor, a novel conveyor system having traffic control gates wherein two puck rotating mechanisms can be incorporated in a single gate operating from a single motor, a novel conveyor system having utility service connected to column supports for the conveyor for convenient access to such utility service and convenient installation of such utility service, and a novel conveyor system that provides common transport of sample tubes to different clinical apparatus and provides for the bypassing of such clinical apparatus if tests are not required at a particular clinical test apparatus.

In view of the above, it will be seen that the several objects of the invention are achieved and other advantageous results obtained.

As various changes can be made in the above constructions without departing from the scope of the invention, it is intended that all matter contained in the above description or shown in the accompanying drawings shall be interpreted as illustrative and not in a limiting sense. 

What is claimed is:
 1. A gating system for a conveyor comprising,a) a gate housing for securement to a conveyor alongside a travel path of the conveyor, b) first and second spaced protractible and retractable control fingers having protracted positions that obstruct the travel path of the conveyor and retracted positions that do not interfere with the flow of traffic on the conveyor, and means on said gate housing for moving said first and second fingers independently of each other along parallel paths into said protracted and retracted positions, c) a first object rotating mechanism provided on said gate housing between said first and second fingers for rotation of a single object on said travel path between said first and second fingers, d) a second object rotating mechanism positioned on said gate housing in series with said first object rotating mechanism, and, e) a third protractible and retractable finger positioned adjacent said second object rotating mechanism, said third finger having protractible and retractable positions and means for moving said third finger into said protracted and retracted positions independently of said first and second fingers to cooperate with said second object rotating mechanism to rotate an object on said travel path.
 2. The gating system as claimed in claim 1 wherein said first and second object rotating mechanisms are controlled by a single drive means.
 3. The gating system as claimed in claim 1 wherein said first, second and third fingers are moveable along parallel paths.
 4. A gating system for a conveyor comprising,a) a gate housing for securement to a conveyor alongside a travel path of the conveyor, b) first and second spaced protractible and retractable control fingers having protracted positions that obstruct the travel path of the conveyor and retracted positions that do not interfere with the flow of traffic on the conveyor, and means on said gate housing for moving said first and second fingers independently of each other along parallel paths into said protracted and retracted positions, c) an object rotating mechanism provided on said gate housing between said first and second fingers for rotation of a single object on said travel path between while confined between said first and second fingers and, d) a third protractible and retractable diversion member positioned adjacent said object rotating mechanism said diversion member having protracted and retracted positions, and means on said gate for moving said diversion member into said protracted and retracted positions independently of said first and second fingers, and said diversion member having an inclined object engaging surface for diverting an object off said travel path by permitting an object to slide relative to the object engaging surface when said diversion member is in one of said protracted and retracted positions.
 5. The gating system as claimed in claim 4 wherein said moving means for said control fingers and said diversion member are pneumatically driven.
 6. The gating system as claimed in claim 4 wherein said diversion member diverts objects off said travel path when said diversion member is in said protracted position. 